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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceOPTIhome Remote Patient Monitoring System
Generic NameImplantable pulse generator
ApplicantImpulse Dynamics (Usa), Inc.
50 Lake Center Executive Pkwy.
401 Rte. 73 N, Bldg. 50 Suite 100
Marlton, NJ 08053
PMA NumberP180036
Supplement NumberS024
Date Received09/05/2023
Decision Date12/01/2023
Product Code QFV 
Advisory Committee Cardiovascular
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
approval for changes to the OPTIhome Remote Patient Monitoring System software for the OPTIMIZER Smart Mini System
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